Incazelo ye-algodystrophy

THEi-algodystrophy, ebizwa nangokuthi " i-reflex sympathetic dystrophy ”Noma” i-tata yesifunda yezinhlungu eziyinkimbinkimbi (SRDC) ”uhlobo lobuhlungu obungapheli obuthinta kakhulu izingalo noma imilenze. Kuyisifo esingajwayelekile. Ubuhlungu buvela ngemva kokuphuka, ukushaywa, ukuhlinzwa noma ukutheleleka.

Izimbangela

Izimbangela ze-algodystrophy zisaqondwa kahle. Kukholakala ukuthi ngokwengxenye kungenxa yokungasebenzi kahle noma ukulimala kwesistimu yezinzwa emaphakathi (ubuchopho nomgogodla) kanye ne-peripheral (imizwa kanye ne-ganglia).

Izimo eziningi zenzeka ngemva kokulimala kwengalo noma umlenze, njengokuphuka noma ukunqunywa. Ukuhlinzwa, ukushaywa, i-sprain noma ngisho nokutheleleka kungabangela i-algodystrophy. Ingozi ye-cerebrovascular (CVA) noma i-myocardial infarction nayo ingaba necala. Ukucindezeleka kungase futhi kusebenze njengesici esibhebhethekisa ubuhlungu obukhulu.

I-Type I algodystrophy, ethinta u-90% wezimo, ivela ngemva kokulimala noma isifo esingathinti imizwa.

I-algodystrophy yohlobo lwe-II ibangelwa ukulimala kwemizwa ezicutshini ezilimele.

Ukuvama

I-Algodystrophy itholakala kunoma iyiphi iminyaka kubantu abadala, ngokwesilinganiso cishe eminyakeni engama-40. Lesi sifo asivamile ukuphatha izingane kanye nabantu abadala.

Lesi sifo sihlasela abesifazane kaningi kunabesilisa. Sikhuluma ngabesifazane aba-3 abathintekile ngowesilisa oyedwa.

Izimpawu ze-algodystrophy

Ngokuvamile, izimpawu zokuqala ze-dystrophy ezivelayo ziyi:

• Ubuhlungu obukhulu noma obuhlabayo obufana nenduku yenaliti kanye nomuzwa ovuthayo engalweni, esandleni, emlenzeni noma onyaweni.
• Ukuvuvukala kwendawo ethintekile.
• Ukuzwela kwesikhumba ukuthinta, ukushisa noma ukubanda.
• Izinguquko ekubunjweni kwesikhumba, esiba mncane, sicwebezele, some futhi sibune endaweni ethintekile.
• Izinguquko ekushiseni kwesikhumba (kubanda noma ukufudumala).

Kamuva, kuvela ezinye izimpawu. Uma sezivele, ngokuvamile azikwazi ukuhlehliswa.

• Izinguquko kumbala wesikhumba osuka kokumhlophe onamabala ukuya kobomvu noma oluhlaza okwesibhakabhaka.
• Izinzipho eziwugqinsi, ezishwabene.
• Ukwanda kokujuluka.
• Ukwanda okulandelwa ukuncipha kwezinwele zesifunda esithintekile.
• Ukuqina, ukuvuvukala kanye nokuwohloka kwamalunga.
• Ukuqina kwemisipha, ubuthakathaka, i-atrophy futhi ngezinye izikhathi ngisho nokuvumelana kwemisipha.
• Ukulahleka kokuhamba endaweni ethintekile.

Ngezinye izikhathi i-algodystrophy ingasakazeka kwenye indawo emzimbeni, njengesitho esiphambene. Ubuhlungu bungakhula ngokucindezeleka.

Kwabanye abantu, izimpawu zingahlala izinyanga noma iminyaka. Kwezinye, bahamba bodwa.

Abantu abasengozini

• I-Algodystrophy ingavela kunoma ibuphi ubudala.
• Abanye abantu bane-genetic predisposition yokudala i-algodystrophy.

Izici zengozi

•     Ukubhema.

Umbono kadokotela wethu